Abstract:
A control system (706) provides automated control of gas washout of a patient interface, such as a mask or nasal prongs. A gas washout vent assembly (60) of the system may include a variable exhaust area such as one defined by overlapping apertures of the assembly or a conduit having a variable gas passage channel. The vent assembly may be formed by nested structures, such as conic or cylindrical members, each having an opening of the overlapping apertures. The vent assembly may be attached substantially near or included with the patient interface. An actuator of the assembly, such as a solenoid or voice coil, manipulates an aperture of the vent assembly. The actuator may be configured for control by a controller to change the exhaust area of the vent assembly based on various methodologies including, for example, sleep detection, disordered breathing event detection, rebreathing volume calculation and/or leak detection.
Abstract:
Systems and/or methods for treating sleep-disordered breathing (SDB) are provided. In particular, systems and/or methods are provided that include software systems for use with auto-titrating devices (e.g. APAP devices) that reduce and/or eliminate the need to calibrate the auto-titrating devices. The software system also may reduce and/or eliminate the need for certain sensors used in such calibrations. Certain example embodiments compute snore based on noises measured during expiration and inspiration, and certain example embodiments set patient leak utilizing the vent flow level. Certain example embodiments change treatment pressure thresholds after measuring patient improvement by monitoring a variable correlated with actual delivery pressure in accordance with an example embodiment, and certain example embodiments provide pressure according to motor speed in accordance with an example embodiment.
Abstract:
A method and apparatus for treating sleep disordered breathing. An arousal index is determined for use in an outer loop of a control algorithm, the arousal index being a measure of the frequency of sleep arousals. The respiratory airflow signal in an inner loop of the control algorithm is monitored to detect an airway obstruction. If the arousal index is high, then the sensitivity of obstruction detection and/or the aggressiveness of the treatment is increased, and if the arousal index is low, then the sensitivity of the obstruction detection and/or the aggressiveness of the treatment is decreased
Abstract:
A low-cost CPAP apparatus in which, upon detection of the transition from inhalation to exhalation, the blower motor is de-energized to allow it to freewheel. When the pressure in the patient mask (or whatever interface is utilized) reaches a minimum pressure level during exhalation, the motor is re-energized and its speed is controlled so to maintain the pressure at a level suitable for exhalation. Upon detection of the transition from exhalation to inhalation, the motor speed is increased to provide higher pressures in the patient mask suitable for inhalation.
Abstract:
A respiratory apparatus comprising a base and removable chamber, wherein the chamber is configured to hold a supply of water and include a blower arrangement adapted to provide a supply of pressurized air or gas to the supply of water. In certain embodiments the respiratory apparatus includes a split motor, wherein the stationary components are located within a base and the rotating portions are located within a chamber.
Abstract:
A device (102) provides respiratory treatment for SDB (including mild OSA) and other respiratory conditions. A flow generator warms and humidifies gas at controlled flow levels. For example, the device (102) delivers breathable gas to the upper airway at flow rates of about 10-35 Liters/minute. Levels of flow rate, temperature and/or humidification of the device may be automatically adjusted in response to the detection of SDB events. The device may also automatically deliver adjustments of any of the levels in accordance with detected phases of respiratory cycles. In some embodiments, the device automatically delivers distinct levels to either of the nares based on independent control of flow to each nare. A warm-up procedure controls temperature and humidity at a desired target during a ramp-up of flow to the set therapy level. A cool-down procedure controls temperature above the dewpoint to avoid condensation internal to the device and patient interface.
Abstract:
A method of using CPAP equipment to sense cardiogenic oscillations in a patient's airflow, and to monitor and treat the patient's cardiac condition. The apparatus diagnoses cardiac morbidity conditions, such as the existence of arrhythmias or other cardiac abnormalities, and influences and optimizes cardiac stroke volume. The apparatus further monitors pulse-transit time, changes in the heart pre-ejection period, and the duration of the cardiac cycle.
Abstract:
A method is disclosed for operating a device that treats sleep disordered breathing (SDB) during successive treatment sessions, where the device provides continuous positive airway pressure during sleep. The method comprises the steps of applying a constant treatment pressure during a first session (20) and deriving a sleep disorder index (SDI) (22) representative of the number of SDB episodes that occurred during the first session. If the treatment pressure should be increased based on the SDI, it is increase during a second, subsequent session (24).
Abstract:
A system for therapy may include a mask (200) for a patient having a frame, cushion, forehead support and a light (100). The mask is connectable to a respiratory treatment apparatus, such as a flow generator, to receive breathable gas for a respiratory therapy. The light may also be connected to the power system and/or control system of the apparatus. A light may also be included in a module, such as a docking station, for a respiratory treatment apparatus. The lights may be controlled by one or more processors, and may be responsive to detected conditions, to assist with therapy. For example, the light may be turned on at a pre-determined time or may be synchronized with the patient's sleep state, to assist in waking up the patient or re-setting the patient's circadian rhythm. Other components, such as sound and aroma generators of the system, may also be controlled for such therapies.
Abstract:
A patient interface includes a mask configured to communicate with at least one airway of a patient, the mask including at least one aperture (402) configured to deliver gas to the at least one airway of the patient; and an airflow resistance member (400) provided to the mask to control the airflow through the at least one airway.